Collaborate with internal departments and investigative clinical research sites to ensure compliance with safety processes.
Qualifications
Bachelor's of Nursing Degree
Broad knowledge of medical terminology
Experience working with or reviewing clinical data, case processing, Clinical experience in a hospital or healthcare setting.
General knowledge of the pharmaceutical industry and Federal Regulations regarding electronic records.
For CSC, Pharmacovigilance experience preferred.
If interested
Apply through with an updated resume. You will be contacted to RSVP for this event.
Medpace Overview
Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries.
Why Medpace?
When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.
Purpose-Driven Work
Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence
Collaborative Culture
Contribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust.
Leadership throughout Medpace is both accessible and approachable
Continuous Growth & Development
Office based environment with on-site mentors
Defined career paths with clear advancement opportunities
Industry renowned onboarding and training programs designed to accelerate professional development
Ongoing training and continuous learning opportunities throughout your career
An environment that encourages employees to influence change, contribute ideas, and grow quickly
Other Employee Benefits
Competitive compensation programs that recognize and reward performance
Comprehensive health, wellness, retirement, and PTO benefits
Office based culture with occasional WFH that provides flexibility for eligible positions after training
Company-sponsored social events
Please note benefits may vary based on country.
What to Expect Next
A Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted.
The core responsibilities of the following roles include
Data Review Associate
Review of clinical data collected in trials
Generate and resolve queries to clarify inconsistent clinical data
Interface with Data Management team to assure query resolution.
Development of clinical review guidelines
Seeking specialization in following therapeutic areas
Oncology
Infectious Disease
Cardiology
Endocrine
Hematology
Clinical Safety Coordinator
Determine plan of action for incoming calls;
Collect, process, and track incoming adverse and serious adverse events;
Write safety narratives;
Report on various safety data; and
Collaborate with internal departments and investigative clinical research sites to ensure compliance with safety processes.
Bachelor's of Nursing Degree
Broad knowledge of medical terminology
Experience working with or reviewing clinical data, case processing, Clinical experience in a hospital or healthcare setting.
General knowledge of the pharmaceutical industry and Federal Regulations regarding electronic records.
For CSC, Pharmacovigilance experience preferred.
If interested
Apply through with an updated resume. You will be contacted to RSVP for this event.
